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Exclusive Breastfeeding Improves Puerperal Glucose Metabolism in Pregnant Women With Gestational Diabetes Mellitus and Links to Lipids Composition

Women's Hospital of Nanjing Medical University

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05629403
Enrollment
84
Registered
2022-11-29
Start date
2021-09-01
Completion date
2022-07-01
Last updated
2022-11-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Feeding, Gestational Diabetes, Lipid Metabolism Disorders

Brief summary

Breastfeeding could effectively be associated with a lower risk of future type 2 diabetes (T2D) in women with gestational diabetes mellitus (GDM), but the short-term protective impact of puerperal breastfeeding on maternal metabolic recovery of GDM women remains unascertained. The investigators recruited GDM participants at 6-9 weeks postpartum and retrieved clinical diagnoses of GDM from electronic medical records. Feeding patterns were collected via phone calls. Glucose metabolism parameters and lipid profiling were performed on fasting plasma samples collected from patients 6-9 weeks postpartum (20 breastfeeding cases vs. 15 formula feeding cases).

Interventions

OTHERobserve

no intervention

Sponsors

Nanjing Medical University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

1. 18-35 years old; 2. gestational age greater than 37 weeks; 3. Body Mass Index (BMI) before pregnancy 18.5-28kg/m2; 4. Have normal listening and speaking skills, can communicate, and are willing to participate in this study.

Exclusion criteria

1. abnormal glucose metabolism or diabetes has been diagnosed before pregnancy; 2. assisted reproduction; 3. GDM patients requiring drug treatment; 4. The use of blood lipid regulation drugs; 5. other pregnancy complications and complications; 6. Suffering from heart, malignant tumor, kidney and other major organ diseases; 7. associated with neurological dysfunction and cognitive impairment; 8. Failure to cooperate with follow-up observers.

Design outcomes

Primary

MeasureTime frameDescription
glucoseAt 6-8 weeks postpartumglucose (mmol/L) determined with human ELISA kits
insulinAt 6-8 weeks postpartuminsulin (mU/L) determined with human ELISA kits
c-peptideAt 6-8 weeks postpartumc-peptide (ng/m) determined with human ELISA kits
HOMA-IRAt 6-8 weeks postpartumfasting glucose and fasting glucose will be combined to report HOMA-IR

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026